Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
  • C09B1/50—Amino-hydroxy-anthraquinones; Ethers and esters thereof
  • C09B1/51—N-substituted amino-hydroxy anthraquinone
  • C09B1/516—N-acylated derivatives
  • C09B1/5165—N-acylated derivatives only amino and hydroxy groups
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
  • Y10S8/93—Pretreatment before dyeing
  • Y10S8/931—Washing or bleaching

Definitions

• the invention also provides a process for the manufacture of these new dyestuffs, wherein a l-hydroxy-Z- amino-anthraquinone, which contains the atomic group- 2 is acylated with a reactive derivative of a mono-carboxylic acid containing at least three carbon atoms.
• acylating agents there are used reactive functional derivatives of mono-carboxylic acids, especially those containing 3-12 carbon atoms.
• reactive functional derivatives of mono-carboxylic acids especially those containing 3-12 carbon atoms.
• aliphatic carboxylic acids such, for example, as propionic acid, butyric acid, isobutyric acid, caproic acid, caprylic acid and lauric acid.
• reactive functional derivatives of cyclic carboxylic acids such as benzoic acid, ptoluic acid or hexahydrobenzoic acid.
• halides advantageously the chlorides
• the acid anhydrides can also be used for the acylation.
• the acylation can be carried out by methods in themselves known, for example, in an inert organic solvent, such as nitrobenzene or chlorobenzene, advantageously with the addition of an acid-binding agent, for example, a tertiary base, such as pyridine or dimethyl-aniline, and is advantageously carried out at a raised temperature.
• an inert organic solvent such as nitrobenzene or chlorobenzene
• an acid-binding agent for example, a tertiary base, such as pyridine or dimethyl-aniline
• the dyestuffs of this invention which contain the grouping of the above Formula 1 and an acyl residue of low molecular weight are very suitable, especially after being suitably pasted, and, if desired, reprecipitated, for example, from sulfuric acid, for dyeing or printing shaped structures and especially fibres of polyesters which consist for example, of alternate glycol and terephthalic acid residues and are known in commerce under the names Terylene or Dacron.
• Pure yellow dyeings which are distinguished by their very good fastness to light, are produced with the dyestuffs of this invention by the usual dyeing methods, for example, from a dye liquor, which contains a dispersion of the dyestuff and advantageously a dispersing agent, at a temperature in the vicinity of 100 C., advantageously with the addition of a swelling agent,-or at a tempera-ture above 100 under superatmospheric pressure.
• the known l-hydroxy-2 acetylamino-anthraquinone can also be used in the presence of a swelling agent for dyeing Terylene; according to the ordinary high temperature process, however, which consists in heating at a temperature above 100 C. the material to be dyed with an aqueous dispersion of the dyestuff in the presence of va wetting agent in a pressure vessel, no'useful dyeings can be obtained.
• the dyestuffs obtained according to the invention which are suitable for the dyeing of Terylene according to both methods represent therefore a surprising step forward in the art as compared with the known l-hydroxy-Z-acetyl-amino anthraquinone.
• the new dyestulfs can also be'used for dyeing or printing shaped structures of cellulose esters or ethers, superpolyamides or superpolyurethanes, and they can alsobe used as pigments;
• mixtures of different hydroxy-acylaminoanthraquinones of this invention can be obtained either by mixing together the finished unitary products or by carrying out the process of this invention with mixtures of different starting materials of the kind referred to above.
• a mixture of different l-hydroxy-Z- aminoanthraquinones may be acylated together, or a mixture of difierent acylating agents may be used, for example, a mixture of propionic acid chloride and butyric acid chloride.
• Mixtures of l-hydroxy-Z-acylaminoanthraquinones with isomeric hydroxy-acylaminoanthraquinones, especially 1-hydroxy-4-acylaminoanthraquinones also give excellent results.
• Example 1 12 parts of l-hydroxy-2-aminoanthraquinone are heated in 36 parts of chlorobenzene with 6.6 parts of dimethylaniline and 6 parts of butyryl chloride until the color of the mixture ceases to change towards yellow. After cooling the reaction mixture, the dyestuif is precipitated with 36 parts of methanol, filtered ofi and washed with methanol. It dyes polyester fibres of the type of Dacron yellow tints having an excellent fastness to light and a good fastness to sublimation.
• Example 2 1.2 parts of the dyestufi' obtained as described in Example 1 are dissolved in 30 parts of sulfuric acid of percent strength at 0 C. and the solution is poured on to ice and water and filtered. The filter cake so obtained is ground with 1 part of dry sulfate cellulose Waste liquor in a roller mill.
• parts of fibrous material of a polyester of the type of Terylene are first cleaned in a bath which contains in 1000 parts of water 1-2 parts of the sodium salt of N-benzyl-a-heptadecyl-benzimidazole-disulfonic acid and 1 part of a concentrated aqueous solution of ammonia for /2 hour.
• the material is then entered into a dyebath in which the dyestuft paste obtained as described in the preceding paragraph has been dispersed with the addition of 4 parts of the sodium salt of N-benzyl- -heptadecylbenzimidazole disulfonic acid.
• the whole is heated in a pressure vessel to C. and maintained for about /2 hour at that temperature.
• Example 3 100 parts of fibrous material of "Ierylene are first cleaned for /2 hour in a bath which contains in 1000 parts of water 1-2 parts of the sodium salt of N-benzyL -heptadecyl-benzimidazole disulfonic acid and 1 part of a concentrated aqueous solution of ammonia. The material is then pro-swelled for /2 hour at 80 C. in a dyebath which contains in 3000 parts of water 15 parts of a mixture of approximately equal parts of orthohydroxydiphenyl, pine oil and Turkey red oil and 15 parts of acetic acid. The bath is then cooled to 50 C.
• Example 2 the dyestuff paste obtained as described in the first paragraph of Example 2 is added.
• the bath is raised to the boil in the course of to hour and dyeing is carried on for 14% hours at a temperature as near as possible to the boiling temperature. then rinsed well and if desired, washed for V2 hour at 6080 C. with a solution which contains in 1000 parts of water 1 part of the sodium salt of N-benzyl- -heptadecylbenzimidazole disulfonic acid. There is obtained a strong yellow dyeing.
• the compound of the formula The material 1s 2.

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• 0
  • BE BE546658D patent/BE546658A/xx unknown
  • BE BE546657D patent/BE546657A/xx unknown
• 1955
  • 1955-04-01 CH CH335548D patent/CH335548A/de unknown
  • 1955-04-01 CH CH333933D patent/CH333933A/de unknown
  • 1955-04-01 CH CH334597D patent/CH334597A/de unknown
• 1956
  • 1956-03-02 FR FR1142261D patent/FR1142261A/fr not_active Expired
  • 1956-03-19 US US572226A patent/US2819274A/en not_active Expired - Lifetime
  • 1956-03-19 US US572225A patent/US2819288A/en not_active Expired - Lifetime
  • 1956-03-22 FR FR1144813D patent/FR1144813A/fr not_active Expired
  • 1956-03-23 FR FR1144817D patent/FR1144817A/fr not_active Expired
  • 1956-03-24 DE DEC12780A patent/DE1063301B/de active Pending
  • 1956-03-26 DE DEC12782A patent/DE1061932B/de active Pending
  • 1956-03-28 GB GB9745/56A patent/GB820402A/en not_active Expired
  • 1956-03-29 GB GB10020/56A patent/GB820448A/en not_active Expired

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